chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1458488915848892GA68GENIChomozygous782089088
1458493045849305AG59GENIChomozygous782089089
1458494455849446AC44GENIChomozygous782089090
1458494765849477GC40GENIChomozygous782089091
1458496305849631CA70GENIChomozygous782089092
1458497515849752CT35GENIChomozygous782089093
1458497825849783CA29GENIChomozygous782089094
1458498385849839GC40GENIChomozygous782089095
1458498535849854CG46GENIChomozygous782089096
1458498725849873CT55GENIChomozygous782089097
1458498855849886AG53GENIChomozygous782089098
1458499095849910TC51GENIChomozygous782089099
1458500305850031CT44GENIChomozygous782089100
1458502395850240GC46GENIChomozygous782089101
1458505225850523GC20GENIChomozygous782089102
1458516825851683AT34GENICheterozygous782089103
1458516905851691CT41GENICheterozygous782089104
1458517545851755CG117GENIChomozygous782089105
1458517975851798TA120GENICheterozygous782089106
1458518105851811GA121GENICheterozygous782089107